Abstract
A common cause of hereditary thrombophilia is activated protein C resistance (APCR), and most cases result from factor V Leiden mutation. An APCR phenotype without association with factor V Leiden has been described. This transversal, observational, nonrandomized study evaluated these 2 phenomena in healthy indigenous and mestizo Mexican subjects (n = 4345), including 600 Mexican natives. No indigenous subjects had APCR, but 82 mestizo subjects did. After retesting, 50 subjects had a negative test. The remaining 32 subjects had factor V Leiden, giving a 0.85% prevalence of factor V Leiden in the mestizo Mexican population. Only 31% of APCR carriers had factor V Leiden. These results show a very low prevalence of APCR and factor V Leiden in Mexico. Except for factor V Leiden, there are no other mutations in the factor V gene responsible for the APCR phenotype. Acquired APCR is nearly twice as prevalent as the inherited variant. © 2008 Sage Publications.
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Majluf-Cruz, A., Moreno-Hernández, M., Ruiz-De-Chávez-Ochoa, A., Monroy-García, R., Majluf-Cruz, K., Guardado-Mendoza, R., … García-Chávez, J. (2008). Activated protein C resistance and factor V Leiden in Mexico. Clinical and Applied Thrombosis/Hemostasis, 14(4), 428–437. https://doi.org/10.1177/1076029607306807
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